ArticleIDCases2026
Early recognition and multidisciplinary care in a pediatric patient with acute infectious purpura fulminans due to MRSA: A rare case report.
Article in IDCases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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0 citing papers in PubMed.
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Acute infectious purpura fulminans (PF) is a rare but life-threatening condition characterized by rapidly progressive purpura, skin necrosis, and disseminated intravascular coagulation. We present a case of a 4-year-old male child who presented with a high-grade fever, maculopapular rash, encephalopathy, and gangrene of distal digits of hands and feet. The child had a tender right submandibular swelling and hepatomegaly. Laboratory findings included leukocytosis (26.48 × 10^9/L), thrombocytopenia (28,000/µL), an elevated C-reactive protein (296 mg/L), and coagulopathy (INR 1.84, D-dimer 540 ng/mL). Imaging revealed submandibular abscess and an extensive infiltrates in the right lower lobe of the lung. Blood culture and pus culture from neck swelling yielded methicillin-resistant
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